Study of Pre Hospital Management of Polytrauma Patients by Medical Teams From a Department in the Parisian Region

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age15+
SponsorCentre Hospitalier Sud Francilien

About this trial

To study the impact of prehospital management duration by SMUR teams in the Essonne department (91) on early patient mortality (within 24 hours) and to analyze the procedures performed on scene.

The study hypothesis is that all-cause in-hospital mortality may be associated with the duration of prehospital care, with either a beneficial impact related to the performance of life-saving interventions or a negative impact due to prolonged time to access definitive treatment.

Identifying potential factors associated with prolonged prehospital management times could help define possible areas for improvement and future interventions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 15 years (upper age limit for the pediatric population)

Severe trauma, defined as any road traffic accident, defenestration, fall from a height greater than 3 meters, stab wound, or ballistic injury requiring medically supervised transport to one of the Level 1 trauma centers in the Île-de-France region

Prehospital management provided by one of the SMUR teams in the Essonne department (91)

Disqualifiers

Patients declared dead at initial medical contact, without resuscitation initiated, or with resuscitation attempted and subsequently discontinued (non-return of spontaneous circulation)

Secondary inter-hospital transfer from another hospital to a Level 1 trauma center

Transport to a hospital for local computed tomography imaging only (without direct admission to a Level 1 trauma center)

Cases regulated (dispatched) by emergency coordination centers other than the Essonne (91) medical dispatch center

Trial population

Patients managed prehospital by a SMUR team from the Essonne department (91) and transported to a Level 1 trauma center according to the predefined inclusion criteria

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

400 Participants
are grouped into 1 trial group
Group A: Patients managed prehospital by a SMUR team from the Essonne department (91) and transported to a Le

Trial outcomes

Primary outcomes

1

Mortality

All-cause in-hospital mortality within 24 hours

Time frame
at day 0

Secondary outcomes

1

Length of hospital stay and neurological outcome

Total duration of hospital stay (in days) and neurological outcome at hospital discharge.

Time frame
Up to one year

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: